Disease

platelet-type bleeding disorder 3

Definition

A blood platelet disease characterized by enhanced binding of von Willebrand factor by the platelet glycoprotein Ib receptor complex that has_material_basis_in mutation in the GP1BA gene on chromosome 17p13.2.

Synonyms

BDPLT3
platelet type-von Willebrand disease

Cross References

ICD10CM:D69.8
MIM:177820

Parent Terms

autosomal dominant disease
blood platelet disease

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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